ReviewEuropean archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery2012
Genetics of hearing loss: where are we standing now?
Review in European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
14 citing papers in PubMed.
- Integrated hearing and genetic screening for neonatal deafness in a resource-limited region: insights from Qingyuan, China.Frontiers in genetics · 2026Article
- [Mutation spectrum analysis of 23-site chip neonatal deafness genetic screening].Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology head and neck surgery · 2024Article
- The genetic basis and the diagnostic yield of genetic testing related to nonsyndromic hearing loss in Qatar.Scientific reports · 2024Article
- Novel pathogenic mutations and further evidence for clinical relevance of genes and variants causing hearing impairment in Tunisian population.Journal of advanced research · 2021Article
- [Analysis of genotypes and hearing phenotypes of mutation infants with deafness].Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology head and neck surgery · 2020Article
- Using the Zebrafish Lateral Line to Understand the Roles of Mitochondria in Sensorineural Hearing Loss.Frontiers in cell and developmental biology · 2020Review
- Successful preimplantation genetic diagnosis by targeted next-generation sequencing on an ion torrent personal genome machine platform.Oncology letters · 2018Article
- Fluvastatin protects cochleae from damage by high-level noise.Scientific reports · 2018Article
- Screening of the SLC17A8 gene as a causative factor for autosomal dominant non-syndromic hearing loss in Koreans.BMC medical genetics · 2016Article
- A missense variant of the ATP1A2 gene is associated with a novel phenotype of progressive sensorineural hearing loss associated with migraine.European journal of human genetics : EJHG · 2015Article
- Genetics of hearing loss in Africans: use of next generation sequencing is the best way forward.The Pan African medical journal · 2015Review
- Hearing impairment and language delay in infants: Diagnostics and genetics.GMS current topics in otorhinolaryngology, head and neck surgery · 2014Review
- Selective ablation of pillar and deiters' cells severely affects cochlear postnatal development and hearing in mice.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2013Article
- Genetic frequencies related to severe or profound sensorineural hearing loss in Inner Mongolia Autonomous Region.Genetics and molecular biologyArticle
Corrections and comments
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Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Hearing loss (HL) is the most common sensory impairment and is caused by a broad range of inherited to environmental causes. Inherited HL consists 50-60% of all HL cases. The inherited form of HL is further classified to different categories. More than 300 syndromes and 40 genes have been identified to result in different levels of HL. Although several diagnostic or screening tests have been developed, yet there are controversies around their use.
Indexed as
Identifiers
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.